7298-73-9

Basic information

• Product Name: 4-ETHOXY-N-METHYLACETANILIDE
• Synonyms: 4-ETHOXY-N-METHYLACETANILIDE;methylphenacetin;n-(4-ethoxyphenyl)-n-methyl-acetamid;n-(4-ethoxyphenyl)-n-methylacetamide;n-methyl-p-acetophenetidid;n-methylphenacetin;N-Methyl-N-(p-ethoxyphenyl)acetamide
• CAS NO: 7298-73-9
• Molecular Formula: C₁₁H₁₅NO₂
• Molecular Weight: 193.2423
• Mol File: 7298-73-9.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 309.1°Cat760mmHg
• Flash Point: 140.8°C
• Appearance: /
• Density: 1.064g/cm³
• Vapor Pressure: 0.000652mmHg at 25°C
• Refractive Index: 1.535
• CAS DataBase Reference: 4-ETHOXY-N-METHYLACETANILIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-ETHOXY-N-METHYLACETANILIDE(7298-73-9)
• EPA Substance Registry System: 4-ETHOXY-N-METHYLACETANILIDE(7298-73-9)

Safety Data

• Hazardous Substances Data: 7298-73-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H15NO2/c1-4-14-11-7-5-10(6-8-11)12(3)9(2)13/h5-8H,4H2,1-3H3

Upstream product

• 156-43-4 4-Ethoxyaniline 
• 103-90-2 4-acetaminophenol 
• 698-69-1 4-chloro-N,N-dimethylaniline 
• 108-24-7 acetic anhydride 
• 1864-93-3 N,N-dimethyl-p-phenetidine 
• 62-44-2 4-ethoxyacetanilide 
• 74-88-4 methyl iodide 
• 3154-18-5 N-methyl-p-phenetidine 
• 75-36-5 acetyl chloride 
• 77-78-1 dimethyl sulfate 

Relevant articles and documents

REMEDIES FOR NEUROPATHIC PAIN

The present invention relates to a compound represented by Formula (I) below: (wherein A represents, for example, phenyl group substituted by R1 and R2, or an unsubstituted furyl group or an unsubstitued thienyl group; R1 represents, for example, hydrogen atom, fluorine atom, chlorine atom, trifluoromethyl group, nitro group, cyano group or methyl group while R2 represents, for example, hydrogen atom; R3 represents, for example, hydrogen atom or methyl group; R4 represents, for example, hydrogen atom or methyl group; R5 represents ethoxy group or isopropoxy group; X represents group: -CH(OH)- or methylene group; and Z represents, for example, a single bond or methylene group unsubstituted or substituted by hydroxyl group), and its salts, and medicinal compositions containing, as their active ingredient, the above compound or its salts. The compound of this invention, which is orally applicable, is highly effective for treating neuroapthic pain while presenting with fewer side-effects than do the conventional analgesics.

Cobalt(II) Chloride Catalyzed Oxidation of 4-Substituted N,N-Dialkylanilines with Molecular Oxygen in the Presence of Acetic Anhydride

The oxidation of 4-substituted N,N-dialkylanilines with molecular oxygen using a catalytic amount of cobalt(II) chloride efficiently proceeds in the presence of acetic anhydride to give N-alkylacetanilides in good yields along with N-alkylformanilides.